A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6362n223



Internal ID22809330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110072601..110096600hg38UCSC Ensembl
chr6:110393804..110417803hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3824000
hg1924000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6613886, nsv6606889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6362n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer